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HRID 45061作成日:2026年10月26日

Imidazole → 3-(tert-Butyl-dimethyl-silanyloxymethyl)-5-trifluoromethyl-phenylamine

https://huagongshe.com/reaction/45061

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物Sodium FluorideHCID 5235—
反応物Ethyl AcetateHCID 8857—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物3-Amino-5-(trifluoromethyl)benzoic acidHCID 609556—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物3-(tert-Butyl-dimethyl-silanyloxymethyl)-5-trifluoromethyl-phenylamineHCID 137329775—

反応条件

温度0 °C

反応手順

To a solution of 3-Amino-5-trifluoromethyl-benzoic acid (2.0 g, 9.76 mmol) in THF (40 mL) at 0° C. is added LiAlH4 in THF (1 M, 39 mL). The mixture is warmed to reflux and stirred for 62 h. The mixture is then cooled to 0° C. and NaF (2.2 g) is added followed by H2O (3.8 mL). The slurry is stirred for 10 minutes and then allowed to warm to rt and stir an additional 40 min. The mixture is filtered and the solid is rinsed with EtOAc and MeOH. The filtrate is concentrated and the crude residue is mixed with imidazole (2.66 g, 39 mmol) and DCM (30 mL) at 0° C. TBSCl (3.5 g, 23.4 mmol) is added and the mixture is stirred at rt for 5 h. The reaction mixture is then diluted with EtOAc, washed with saturated aqueous NaHCO3, brine, and dried over Na2SO4. Concentration provides the title compound that is carried on to next step without further purification. MS (ESI) m/z 306.1 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541432B2
出典データセットuspto-grants-2013_09
ORD IDord-1875c82f897145ed8ba3994b007c15ee
出典メモuspto-grants-2013_09